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RDH5 Antikörper

RDH5 Reaktivität: Human, Maus, Ratte IF Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN6571537
  • Target Alle RDH5 Antikörper anzeigen
    RDH5 (Retinol Dehydrogenase 5 (11-Cis/9-Cis) (RDH5))
    Reaktivität
    Human, Maus, Ratte
    Wirt
    • 6
    • 1
    • 1
    Kaninchen
    Klonalität
    • 8
    Polyklonal
    Konjugat
    • 8
    Dieser RDH5 Antikörper ist unkonjugiert
    Applikation
    • 4
    • 4
    • 4
    • 3
    • 1
    • 1
    Immunofluorescence (IF)
    Aufreinigung
    Affinity purification
    Immunogen
    Recombinant fusion protein of human RDH5 (NP_002896.2).
    Isotyp
    IgG
    Top Product
    Discover our top product RDH5 Primärantikörper
  • Applikationshinweise
    IF 1:50-1:100
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    RDH5 (Retinol Dehydrogenase 5 (11-Cis/9-Cis) (RDH5))
    Andere Bezeichnung
    RDH5 (RDH5 Produkte)
    Synonyme
    9cRDH antikoerper, HSD17B9 antikoerper, RDH1 antikoerper, SDR9C5 antikoerper, RDHB antikoerper, MGC84134 antikoerper, RDH5 antikoerper, rdh1 antikoerper, hsd17b9 antikoerper, im:6901729 antikoerper, si:dkey-102c8.5 antikoerper, 9-cis antikoerper, AI987873 antikoerper, RDH4 antikoerper, cRDH antikoerper, retinol dehydrogenase 5 antikoerper, retinol dehydrogenase 1 antikoerper, retinol dehydrogenase 5 L homeolog antikoerper, retinol dehydrogenase 5 (11-cis/9-cis) antikoerper, RDH5 antikoerper, rdh1 antikoerper, rdh5.L antikoerper, rdh5 antikoerper, Rdh5 antikoerper
    Hintergrund
    This gene encodes an enzyme belonging to the short-chain dehydrogenases/reductases (SDR) family. This retinol dehydrogenase functions to catalyze the final step in the biosynthesis of 11-cis retinaldehyde, which is the universal chromophore of visual pigments. Mutations in this gene cause autosomal recessive fundus albipunctatus, a rare form of night blindness that is characterized by a delay in the regeneration of cone and rod photopigments. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the neighboring upstream BLOC1S1 (biogenesis of lysosomal organelles complex-1, subunit 1) gene.
    Molekulargewicht

    Observed_MW: 38kDa

    Calculated_MW: 34kDa

    Gen-ID
    5959
    UniProt
    Q92781
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